<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miyashima S</submitter><funding>European Research Council</funding><funding>Medical Research Council</funding><funding>Dutch Research Council (NWO)</funding><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>490-494</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7617008</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>565(7740)</volume><pubmed_abstract>Apical growth in plants initiates upon seed germination, whereas radial growth is primed only during early ontogenesis in procambium cells and activated later by the vascular cambium&lt;sup>1&lt;/sup>. Although it is not known how radial growth is organized and regulated in plants, this system resembles the developmental competence observed in some animal systems, in which pre-existing patterns of developmental potential are established early on&lt;sup>2,3&lt;/sup>. Here we show that in Arabidopsis the initiation of radial growth occurs around early protophloem-sieve-element cell files of the root procambial tissue. In this domain, cytokinin signalling promotes the expression of a pair of mobile transcription factors-PHLOEM EARLY DOF 1 (PEAR1) and PHLOEM EARLY DOF 2 (PEAR2)-and their four homologues (DOF6, TMO6, OBP2 and HCA2), which we collectively name PEAR proteins. The PEAR proteins form a short-range concentration gradient that peaks at protophloem sieve elements, and activates gene expression that promotes radial growth. The expression and function of PEAR proteins are antagonized by the HD-ZIP III proteins, well-known polarity transcription factors&lt;sup>4&lt;/sup>-the expression of which is concentrated in the more-internal domain of radially non-dividing procambial cells by the function of auxin, and mobile miR165 and miR166 microRNAs. The PEAR proteins locally promote transcription of their inhibitory HD-ZIP III genes, and thereby establish a negative-feedback loop that forms a robust boundary that demarks the zone of cell division. Taken together, our data establish that during root procambial development there exists a network in which a module that links PEAR and HD-ZIP III transcription factors integrates spatial information of the hormonal domains and miRNA gradients to provide adjacent zones of dividing and more-quiescent cells, which forms a foundation for further radial growth.</pubmed_abstract><journal>Nature</journal><pubmed_title>Mobile PEAR transcription factors integrate positional cues to prime cambial growth.</pubmed_title><pmcid>PMC7617008</pmcid><funding_grant_id>864.13.001</funding_grant_id><funding_grant_id>MR/M008975/1</funding_grant_id><funding_grant_id>323052</funding_grant_id><funding_grant_id>BB/N013158/1</funding_grant_id><funding_grant_id>BB/L023555/1</funding_grant_id><funding_grant_id>BB/M019837/1</funding_grant_id><pubmed_authors>Helariutta Y</pubmed_authors><pubmed_authors>Wallner ES</pubmed_authors><pubmed_authors>Greb T</pubmed_authors><pubmed_authors>Miyashima S</pubmed_authors><pubmed_authors>Roszak P</pubmed_authors><pubmed_authors>Mellor N</pubmed_authors><pubmed_authors>Sevilem I</pubmed_authors><pubmed_authors>Hooiveld G</pubmed_authors><pubmed_authors>De Rybel B</pubmed_authors><pubmed_authors>Melnyk CW</pubmed_authors><pubmed_authors>Help-Rinta-Rahko H</pubmed_authors><pubmed_authors>Sozzani R</pubmed_authors><pubmed_authors>Blob B</pubmed_authors><pubmed_authors>Mahonen AP</pubmed_authors><pubmed_authors>Smetana O</pubmed_authors><pubmed_authors>Hashimoto K</pubmed_authors><pubmed_authors>Bishopp A</pubmed_authors><pubmed_authors>Nakajima K</pubmed_authors><pubmed_authors>Siligato R</pubmed_authors><pubmed_authors>Heo JO</pubmed_authors><pubmed_authors>Smet W</pubmed_authors><pubmed_authors>Boekschoten M</pubmed_authors><pubmed_authors>Otero S</pubmed_authors><pubmed_authors>Kondo Y</pubmed_authors><pubmed_authors>Toyokura K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mobile PEAR transcription factors integrate positional cues to prime cambial growth.</name><description>Apical growth in plants initiates upon seed germination, whereas radial growth is primed only during early ontogenesis in procambium cells and activated later by the vascular cambium&lt;sup>1&lt;/sup>. Although it is not known how radial growth is organized and regulated in plants, this system resembles the developmental competence observed in some animal systems, in which pre-existing patterns of developmental potential are established early on&lt;sup>2,3&lt;/sup>. Here we show that in Arabidopsis the initiation of radial growth occurs around early protophloem-sieve-element cell files of the root procambial tissue. In this domain, cytokinin signalling promotes the expression of a pair of mobile transcription factors-PHLOEM EARLY DOF 1 (PEAR1) and PHLOEM EARLY DOF 2 (PEAR2)-and their four homologues (DOF6, TMO6, OBP2 and HCA2), which we collectively name PEAR proteins. The PEAR proteins form a short-range concentration gradient that peaks at protophloem sieve elements, and activates gene expression that promotes radial growth. The expression and function of PEAR proteins are antagonized by the HD-ZIP III proteins, well-known polarity transcription factors&lt;sup>4&lt;/sup>-the expression of which is concentrated in the more-internal domain of radially non-dividing procambial cells by the function of auxin, and mobile miR165 and miR166 microRNAs. The PEAR proteins locally promote transcription of their inhibitory HD-ZIP III genes, and thereby establish a negative-feedback loop that forms a robust boundary that demarks the zone of cell division. Taken together, our data establish that during root procambial development there exists a network in which a module that links PEAR and HD-ZIP III transcription factors integrates spatial information of the hormonal domains and miRNA gradients to provide adjacent zones of dividing and more-quiescent cells, which forms a foundation for further radial growth.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2026-06-02T03:42:50.308Z</modification><creation>2025-04-04T01:57:52.37Z</creation></dates><accession>S-EPMC7617008</accession><cross_references><pubmed>30626969</pubmed><doi>10.1038/s41586-018-0839-y</doi></cross_references></HashMap>